Département des Neurosciences Cliniques, CHUV, University of Lausanne, Switzerland.
Brain. 2010 Dec;133(Pt 12):3661-75. doi: 10.1093/brain/awq300. Epub 2010 Nov 10.
Tourette syndrome is a childhood-onset neuropsychiatric disorder with a high prevalence of attention deficit hyperactivity and obsessive-compulsive disorder co-morbidities. Structural changes have been found in frontal cortex and striatum in children and adolescents. A limited number of morphometric studies in Tourette syndrome persisting into adulthood suggest ongoing structural alterations affecting frontostriatal circuits. Using cortical thickness estimation and voxel-based analysis of T1- and diffusion-weighted structural magnetic resonance images, we examined 40 adults with Tourette syndrome in comparison with 40 age- and gender-matched healthy controls. Patients with Tourette syndrome showed relative grey matter volume reduction in orbitofrontal, anterior cingulate and ventrolateral prefrontal cortices bilaterally. Cortical thinning extended into the limbic mesial temporal lobe. The grey matter changes were modulated additionally by the presence of co-morbidities and symptom severity. Prefrontal cortical thickness reduction correlated negatively with tic severity, while volume increase in primary somatosensory cortex depended on the intensity of premonitory sensations. Orbitofrontal cortex volume changes were further associated with abnormal water diffusivity within grey matter. White matter analysis revealed changes in fibre coherence in patients with Tourette syndrome within anterior parts of the corpus callosum. The severity of motor tics and premonitory urges had an impact on the integrity of tracts corresponding to cortico-cortical and cortico-subcortical connections. Our results provide empirical support for a patho-aetiological model of Tourette syndrome based on developmental abnormalities, with perturbation of compensatory systems marking persistence of symptoms into adulthood. We interpret the symptom severity related grey matter volume increase in distinct functional brain areas as evidence of ongoing structural plasticity. The convergence of evidence from volume and water diffusivity imaging strengthens the validity of our findings and attests to the value of a novel multimodal combination of volume and cortical thickness estimations that provides unique and complementary information by exploiting their differential sensitivity to structural change.
妥瑞氏症是一种儿童期起病的神经精神疾病,伴有注意力缺陷多动障碍和强迫症的高患病率。在儿童和青少年中发现了额叶皮层和纹状体的结构变化。在持续到成年的妥瑞氏症中,进行了少量的形态计量学研究,表明影响额纹状体回路的持续结构改变。我们使用皮质厚度估计和 T1 和弥散加权结构磁共振成像的体素分析,比较了 40 名妥瑞氏症患者和 40 名年龄和性别匹配的健康对照者。妥瑞氏症患者双侧眶额、前扣带回和腹外侧前额皮质的灰质体积减少。皮质变薄延伸到边缘内侧颞叶。灰质变化还受到共病和症状严重程度的调节。前额皮质厚度的减少与抽动严重程度呈负相关,而初级体感皮层的体积增加取决于预感感觉的强度。眶额皮层体积变化与灰质内异常的水弥散性进一步相关。白质分析显示,妥瑞氏症患者在前连合的前部存在纤维连贯性变化。运动性抽动和预感冲动的严重程度影响与皮质-皮质和皮质-皮质下连接对应的束的完整性。我们的研究结果为基于发育异常的妥瑞氏症的病理发病机制模型提供了经验支持,代偿系统的破坏标志着症状持续到成年。我们将不同功能脑区与症状严重程度相关的灰质体积增加解释为持续结构可塑性的证据。体积和水弥散成像的证据的收敛性增强了我们发现的有效性,并证明了体积和皮质厚度估计的新型多模态组合的价值,该组合通过利用其对结构变化的不同敏感性提供了独特和互补的信息。